Fatty acid metabolism in Saccharomyces cerevisiae von van Roermund, C W T, Waterham, H R, Ijlst, L, Wanders, R J A

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Proteasome-dependent protein quality control of the peroxisomal membrane protein Pxa1p von Devarajan, S., Meurer, M., van Roermund, C.W.T., Chen, X., Hettema, E.H., Kemp, S., Knop, M., Williams, C.

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Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of d-Bifunctional Protein von Ferdinandusse, S., van Grunsven, E.G., Oostheim, W., Denis, S., Hogenhout, E.M., IJlst, L., van Roermund, C.W.T., Waterham, H.R., Goldfischer, S., Wanders, R.J.A.

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Identification of human PMP34 as a peroxisomal ATP transporter von Visser, W.F, van Roermund, C.W.T, Waterham, H.R, Wanders, R.J.A

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The inborn errors of peroxisomal β‐oxidation: A review von Wanders, R. J. A., Roermund, C. W. T., Schutgens, R. B. H., Barth, P. G., Heymans, H. S. A., Bosch, H., Tager, J. M.

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X‐linked adrenoleukodystrophy: Biochemical diagnosis and enzyme defect von Wanders, R. J. A., Roermund, C. W. T., Lageweg, W., Jakobs, B. S., Schutgens, R. B. H., Nijenhuis, A. A., Tager, J. M.

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Bifunctional enzyme deficiency: Identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal β‐oxidation of unknown aetiology by means of com... von Wanders, R. J. A., Roermund, C. W. T., Brul, S., Schutgens, R. B. H., Tager, J. M.

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Identification of pristanoyl‐CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: Implications for Zellweger syndrome von Wanders, R. J. A., Roermund, C. W. T., Jakobs, C., Brink, H. J.

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Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2‐ketophytanic acid from 2‐hydroxyphytanic acid and its deficiency in the Zellweger syndr... von Wanders, R. J. A., Roermund, C. W. T., Schor, D. S. M., Brink, H. J., Jakobs, C.

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Di‐ and trihydroxycholestanoic acidaemia with hepatic failure von Przyrembel, H., Wanders, R. J. A., Roermund, C. W. T., Schutgens, R. B. H., Mannaerts, G. P., Casteels, M.

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A bifunctional protein with deficient enzymic activity: Identification of a new peroxisomal disorder using novel methods to measure the peroxisomal β‐oxidation enzyme activities von Wanders, R. J. A., Roermund, C. W. T., Schelen, A., Schutgens, R. B. H., Tager, J. M., Stephenson, J. B. P., Clayton, P. T.

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X‐linked adrenoleukodystrophy: Identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl‐CoA synthetase using a newly developed method... von Wanders, R. J. A., Roermund, C. W. T., Wijland, M. J. A., Schutgens, R. B. H., Schram, A. W., Tager, J. M., Bosch, H., Schalkwijk, C.

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Di‐ and trihydroxycholestanaemia in twin sisters von Wanders, R. J. A., Roermund, C. W. T., Schelen, A., Schutgens, R. B. H., Zeman, J., Kozich, V., Hyanek, J., Casteels, M., Mannaerts, G. P.

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A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy) von BWEE TIEN POLL-THE, ROELS, F, TAGER, J. M, SAUDUBRAY, J.-M, OGIER, H, SCOTTO, J, VAMECQ, J, SCHUTGENS, R. B. H, WANDERS, R. J. A, VAN ROERMUND, C. W. T, VAN WIJLAND, M. J. A, SCHRAM, A. W

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Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia von Wanders, R. J. A., Roermund, C. W. T., Wijland, M. J. A., Schutgens, R. B. H., Tager, J. M., Bosch, H., Thomas, G. H.

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Measurement of peroxisomal fatty acid β‐oxidation in cultured human skin fibroblasts von Wanders, R. J. A., Denis, S., Ruiter, J. P. N., Schutgens, R. B. H., Roermund, C. W. T., Jacobs, B. S.

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Deficient oxidation of trihydroxycoprostanic acid in liver homogenates from patients with peroxisomal diseases von Casteels, M., Van Roermund, C. W. T., Schepers, L., Govaert, L., Eyssen, H. J., Mannaerts, G. P., Wanders, R. J. A.

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Human Peroxisomal 3-oxoacyl-coenzyme A Thiolase Deficiency von Schram, André W., Goldfischer, Sidney, Carlo W. T. Van Roermund, Brouwer-Kelder, Elisabeth M., Collins, Janna, Hashimoto, Takashi, Hugo S. A. Heymans, Van Den Bosch, Henk, Ruud B. H. Schutgens, Tager, Joseph M., Ronald J. A. Wanders

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Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long... von Wanders, R.J.A., van Roermund, C.W.T., van Wijland, M.J.A., Schutgens, R.B.H., van den Bosch, H., Schram, A.W., Tager, J.M.

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Metabolic Aspects of Peroxisomal Disorders von WANDERS, R. J. A., JANSEN, G., van ROERMUND, C. W. T., DENIS, S., SCHUTGENS, R. B. H., JAKOBS, B. S.

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